Abstract

BackgroundCancer stem cells (CSCs) have been recognized as an important drug target, however, the underlying mechanisms have not been fully understood. SKP1 is a traditional drug target for cancer therapy, while, whether SKP1 promotes colorectal cancer (CRC) stem cells (CRC-SCs) and the underlying mechanisms have remained elusive.MethodsHuman CRC cell lines and primary human CRC cells were used in this study. Gene manipulation was performed by lentivirus system. The mRNA and protein levels of target genes were examined by qRT-PCR and western blot. The sphere-forming and in vitro migration capacities were determined by sphere formation and transwell assay. The self-renewal was determined by limiting dilution assay. The tumorigenicity and metastasis of cancer cells were examined by xenograft model. The promoter activity was examined by luciferase reporter assay. Nuclear run-on and Chromatin immunoprecipitation-PCR (ChIP-PCR) assay were employed to examine the transcription and protein-DNA interaction. Co-immunoprecipitation assay was used to test protein–protein interaction. The relationship between gene expression and survival was analyzed by Kaplan–meier analysis. The correlation between two genes was analyzed by Spearman analysis. Data are represented as mean ± SD and the significance was determined by Student’s t test.ResultsSKP1 was upregulated in CRC-SCs and predicted poor prognosis of colon cancer patients. Overexpression of SKP1 promoted the stemness of CRC cells reflected by increased sphere-forming, migration and self-renewal capacities as well as the expression of CSCs markers. In contrast, SKP1 depletion produced the opposite effects. SKP1 strengthened YAP activity and knockdown of YAP abolished the effect of SKP1 on the stemness of CRC cells. SKP1 suppressed RASSF1 at both mRNA and protein level. Overexpression of RASSF1 abolished the effect of SKP1 on YAP activity and CRC stemness.ConclusionOur results demonstrated that SKP1 suppresses RASSF1 at both mRNA and protein level, attenuates Hippo signaling, activates YAP, and thereby promoting the stemness of CRC cells.

Highlights

  • Cancer stem cells (CSCs) have been recognized as an important drug target, the underlying mechanisms have not been fully understood

  • S-Phase Kinase Associated Protein 1 (SKP1) is associated with the stemness of colorectal cancer (CRC) cells CSCs possess the ability to form three-dimensional spheres in suspension culture condition [7,8,9]

  • To investigate whether SKP1 is associated with the stemness of CRC stem cells (CRC-SCs), we first examined the relative mRNA expression level of SKP1 in adherent, suspension cultured sphere and re-adherent CRC cells

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Summary

Introduction

Cancer stem cells (CSCs) have been recognized as an important drug target, the underlying mechanisms have not been fully understood. SKP1 is a traditional drug target for cancer therapy, while, whether SKP1 promotes colorectal cancer (CRC) stem cells (CRC-SCs) and the underlying mechanisms have remained elusive. Tian et al Cancer Cell Int (2020) 20:579 the improvement of our understanding about the underlying mechanisms is urgently needed. As the mechanisms underlying the maintenance of cancer stemness have not been fully understood, few strategies eradicating CSCs have been developed. Exploring novel mechanisms and identifying novel drug targets are important to achieve this goal

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